Muscle cells challenged with saturated fatty acids mount an autonomous inflammatory response that activates macrophages
- Nicolas J PillonAffiliated withProgram in Cell Biology, The Hospital for Sick Children
- , Karen AraneAffiliated withProgram in Cell Biology, The Hospital for Sick Children
- , Philip J BilanAffiliated withProgram in Cell Biology, The Hospital for Sick Children
- , Tim T ChiuAffiliated withProgram in Cell Biology, The Hospital for Sick Children
- , Amira KlipAffiliated withProgram in Cell Biology, The Hospital for Sick Children Email author
Obesity is associated with chronic low-grade inflammation. Within adipose tissue of mice fed a high fat diet, resident and infiltrating macrophages assume a pro-inflammatory phenotype characterized by the production of cytokines which in turn impact on the surrounding tissue. However, inflammation is not restricted to adipose tissue and high fat-feeding is responsible for a significant increase in pro-inflammatory cytokine expression in muscle. Although skeletal muscle is the major disposer of dietary glucose and a major determinant of glycemia, the origin and consequence of muscle inflammation in the development of insulin resistance are poorly understood.
We used a cell culture approach to investigate the vectorial crosstalk between muscle cells and macrophages upon exposure to physiological, low levels of saturated and unsaturated fatty acids. Inflammatory pathway activation and cytokine expression were analyzed in L6 muscle cells expressing myc-tagged GLUT4 (L6GLUT4myc) exposed to 0.2 mM palmitate or palmitoleate. Conditioned media thereof, free of fatty acids, were then tested for their ability to activate RAW264.7 macrophages.
Palmitate -but not palmitoleate- induced IL-6, TNFα and CCL2 expression in muscle cells, through activation of the NF-κB pathway. Palmitate (0.2 mM) alone did not induce insulin resistance in muscle cells, yet conditioned media from palmitate-challenged muscle cells selectively activated macrophages towards a pro-inflammatory phenotype.
These results demonstrate that low concentrations of palmitate activate autonomous inflammation in muscle cells to release factors that turn macrophages pro-inflammatory. We hypothesize that saturated fat-induced, low-grade muscle cell inflammation may trigger resident skeletal muscle macrophage polarization, possibly contributing to insulin resistance in vivo.
KeywordsInflammation Muscle Palmitate Palmitoleate Saturated fat Obesity Insulin resistance GLUT4 Glucose uptake
- Muscle cells challenged with saturated fatty acids mount an autonomous inflammatory response that activates macrophages
- Open Access
- Available under Open Access This content is freely available online to anyone, anywhere at any time.
Cell Communication and Signaling
- Online Date
- October 2012
- Online ISSN
- BioMed Central
- Additional Links
- Saturated fat
- Insulin resistance
- Glucose uptake